Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs10786610 10 100880906 TF binding site variant G/C;T snv 1
rs10789181
DNAJC6
1 65350884 intron variant A/G snv 0.72 1
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs10810071
LOC101929507
9 13992264 downstream gene variant C/T snv 0.19 1
rs10816359
LINC01505
9 105995389 intron variant T/G snv 0.18 1
rs10817638
LOC105376229
9 114560262 regulatory region variant A/G snv 0.37 1
rs10820310 9 102923803 downstream gene variant A/G snv 0.28 1
rs10857036
NDST4
4 115075517 intron variant T/C snv 0.44 1
rs10860153 12 97147754 intron variant A/G snv 0.36 1
rs10861880
LOC105369965 ; WSCD2
12 108217697 intron variant T/C snv 0.44 1
rs10867332
KRT18P24
9 79036617 non coding transcript exon variant G/C snv 0.34 1
rs10870546
MUC8
12 132478023 intergenic variant A/G snv 0.63 1
rs10874340 1 82793397 intron variant G/A;T snv 1
rs10895140
TRPC6
11 101565990 intron variant A/G snv 0.62 1
rs10895141
TRPC6
11 101566010 intron variant A/C;T snv 0.62 1
rs10899489
GAB2
11 78384327 non coding transcript exon variant C/A;T snv 1
rs10902475
LOC107984455
12 131925700 intron variant C/A snv 0.57 1
rs10908948 9 89806050 intron variant G/A snv 0.41 1
rs10913213
PAPPA2
1 176594124 intron variant C/G snv 0.32 1
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs10940138 5 67898641 intron variant C/T snv 0.21 1
rs10941225 5 34961375 downstream gene variant T/A snv 0.32 1
rs10960303 9 11839805 intron variant C/A snv 0.19 1